TWI290341B - Method of fabricating a coated process chamber component - Google Patents
Method of fabricating a coated process chamber component Download PDFInfo
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- TWI290341B TWI290341B TW091134128A TW91134128A TWI290341B TW I290341 B TWI290341 B TW I290341B TW 091134128 A TW091134128 A TW 091134128A TW 91134128 A TW91134128 A TW 91134128A TW I290341 B TWI290341 B TW I290341B
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- Prior art keywords
- component
- ceramic body
- assembly
- coating
- process chamber
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Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/32—Gas-filled discharge tubes
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
- C04B41/50—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials
- C04B41/51—Metallising, e.g. infiltration of sintered ceramic preforms with molten metal
- C04B41/515—Other specific metals
- C04B41/5155—Aluminium
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/80—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
- C04B41/81—Coating or impregnation
- C04B41/85—Coating or impregnation with inorganic materials
- C04B41/88—Metals
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/22—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
- C23C14/56—Apparatus specially adapted for continuous coating; Arrangements for maintaining the vacuum, e.g. vacuum locks
- C23C14/564—Means for minimising impurities in the coating chamber such as dust, moisture, residual gases
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/02—Pretreatment of the material to be coated, e.g. for coating on selected surface areas
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/04—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
- C23C4/06—Metallic material
- C23C4/08—Metallic material containing only metal elements
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C4/00—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
- C23C4/12—Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the method of spraying
- C23C4/131—Wire arc spraying
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Ceramic Engineering (AREA)
- Plasma & Fusion (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Metallurgy (AREA)
- Mechanical Engineering (AREA)
- Structural Engineering (AREA)
- Inorganic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Physical Vapour Deposition (AREA)
- Drying Of Semiconductors (AREA)
- Coating By Spraying Or Casting (AREA)
- Chemically Coating (AREA)
Abstract
Description
1290341 九、發明說明 發明所屬之技術領域】 本發明之實施例係關於 法 種製造製程處^組件之方 【先前技術】 一基板製程處理室係在—數發之製程氣趙中處理一基 板以製作電路,其中該氣體諸如^ 路晶片與顯示器。該製程處理室:i電路諸如積體電 至一般包含一圍繞眛 栌 激發器、與一排放系統,其中讀圍 回、一·; 飞園繞牆係圍繞住一域 以供製程氣體導入於内,該氣體/ 裏程L域 瑕教發器係激發該製體, 而該排放系統係排放與控制處理~ 狀體 ,^ 至内之製程氣體壓力。該製 程處理室之使用係如沉積材料 ^ n ^ ^ 丁叶於一基板上或自一其扨卜飩 刻材料。舉例而言,處理室係用 基板上触 β於濺鍍沉積一材粗你姑I把 上,其中該材料諸如鋁、銅或钽 4於該基板 氮化鈦等之金屬化合物。、專之金屬’或諸如氮化组或 暴露於處理至中之處理室組件常塗覆有一塗層 係用以增強濺鍍材料於該塗屛μ * 丈層 乂踅層上之附著力,並增加該下 料在處理室中對電漿之抗腐斜从 3材 沉腐蝕性,或用以提供其他欲求之槌 質,如具導電性表面,其中 Τ處理至組件係諸如處理室側脾、 頂板、襯墊、或沉積環之矣二 . m 頁衣之表面。舉例而言,一處理室組 由氧化鋁或石英材料所劁供 ^ 衣爾,並可以電漿分散而加以塗 鋁塗層。 在製造此組件之製鞋士 , 1程中,組件之陶瓷體的製備,係先採 1290341 以處理該組件,繼之沈 用向能量喷砂(grit blasting )步驟加 其中該酸性溶液係如具有高 驟係用於在再磨光製程中去 浸該組件於濃縮之酸性溶液中, 於20%濃度之HF溶液。噴砂步 除既存之組件塗層’或用於製備該级件之表面以接受新的塗 層,且其係使已處理之組件表面,達到大於2(^微英对之高 表面粗糙平均(Ra)值。咸信較高之粗糙度值對於在陶瓷體上 之上方塗層提供較佳之附著力。故此之後該組件係在一再 磨光製程情形中施以再塗覆’或在—新組件情形中施以新的BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for manufacturing a manufacturing process. [Prior Art] A substrate processing chamber processes a substrate in a process of several processes. A circuit is fabricated in which the gas is such as a wafer and a display. The process chamber: an i circuit, such as an integrated circuit, generally includes a surrounding 眛栌 exciter, and an exhaust system, wherein the readback is repeated, and the fly garden surrounds a domain for the process gas to be introduced therein. The gas/mileage L-domain 瑕 发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发 激发The processing chamber is used, for example, to deposit a material on a substrate or to etch material from a substrate. For example, the processing chamber is formed by sputtering a substrate on the substrate by sputtering, wherein the material is a metal compound such as aluminum, copper or tantalum on the substrate such as titanium nitride. a special metal' or a process chamber assembly such as a nitrided group or exposed to a process is often coated with a coating to enhance the adhesion of the sputter material to the coated layer. Increasing the anti-corrosion of the plasma in the processing chamber from the 3 material corrosion corrosiveness, or to provide other desired enamel, such as a conductive surface, wherein the enamel treatment to the component system such as the treatment chamber side spleen, The top surface, the liner, or the surface of the deposition ring. For example, a chamber group is made of alumina or quartz material and coated with aluminum and coated with aluminum. In the manufacture of the shoemaker of this assembly, in the first step, the preparation of the ceramic body of the component is firstly carried out by 1239041 to process the component, followed by the step of adding grit blasting to the step of adding the acidic solution. The high sequence is used to de-immerse the module in a concentrated acidic solution in a 20% strength HF solution during the re-polishing process. The blasting step removes the existing component coating' or is used to prepare the surface of the grade to accept a new coating, and it is such that the surface of the treated component is greater than 2 (a micro-inferior high surface roughness average (Ra) The higher roughness value provides better adhesion to the upper coating on the ceramic body. Therefore, the component is then recoated or in the case of a new component in a re-polishing process. Apply new
塗層。 然而,此類傳統製造組件之方法,仍常導致組件具有無 法接受之低零件壽命,故需經常性地置換或再磨光該組件。 舉例而g,當使用此類組件於PVD製程中以自靶材濺鍍沉積 材料於一基板上時,該濺鍍材料係也累積於組件之表面上。 該累積之沉積物係可引起熱膨脹應力,導致置於下方之塗層 自陶究體上分層、剝離、與分片剝落。處理室中之電漿係可 擴散至塗層之剝離處或其他損傷之區域,並腐蝕該組件之暴 露表面,最終導致組件故障。coating. However, such conventional methods of fabricating components often result in components having unacceptably low component life, requiring frequent replacement or re-polishing of the components. For example, when such a component is used in a PVD process to deposit material onto a substrate from a target sputter, the sputter material also accumulates on the surface of the component. The accumulated deposits can cause thermal expansion stress, causing the underlying coating to delaminate, peel, and flaking from the ceramic body. The plasma in the processing chamber can diffuse to the strip or other damaged areas of the coating and corrode the exposed surface of the assembly, ultimately causing component failure.
故此,希冀具有一製程,該製程係具有在一基板製程環 境中’製造具有欲求之表面性質之組件的能力。更希冀具有 一組件’其在可能沉積有過量濺鑛材料於組件上之製程中, 係具有良好的使用期,並可沉積過量濺鍍材料於該組件上。 同樣也希冀在該組件於操作過程中性質產生惡化時,視其需 求施以再磨光步驟。 6 1290341 【發明内容】 一種製造於製程 - 少包含具有晶粒與晶界區域的陶曼體,且該方法至少包含下 列步驟: (a)珠擊該組件,以提供具有粗缝度平均值低於1 $〇微英 对之一表面;Accordingly, it is desirable to have a process that has the ability to fabricate components having desirable surface properties in a substrate processing environment. It is even more desirable to have a component that has a good lifetime in the process of depositing excess sputter material onto the component and depositing excess sputter material onto the component. It is also desirable to apply a refurbishing step as needed when the component deteriorates during operation. 6 1290341 SUMMARY OF THE INVENTION A process for manufacturing a process - containing a ceramic body having a grain and a grain boundary region, and the method comprises at least the following steps: (a) beating the component to provide a low average value of the rough seam On a surface of 1 $〇微英;
(b)沈浸該組件於一溶液中,其中該溶液係具有充分低濃 度的酸或鹼,以減少該陶瓷體之晶界區域之蝕刻;及 (e)於該陶瓷體之至少一部分上形成一金屬塗層。 一種製造使用於製程處理室之一組件的方法,該組件至 少包含具有氧化鋁晶粒與晶界區域的陶瓷體,且該方法至少 包含下列步驟: (a) 珠擊該組件,以提供具有粗糙度平均值低於15()微英 忖之一表面粗链度; (b) 沈浸該組件於一溶液中,其中該溶液係包含濃度低於 約10體積百分比的HF、HC1與HN〇3之一或多者;及(b) immersing the component in a solution, wherein the solution has a sufficiently low concentration of acid or base to reduce etching of the grain boundary region of the ceramic body; and (e) forming a portion on at least a portion of the ceramic body Metal coating. A method of fabricating an assembly for use in a process chamber, the assembly comprising at least a ceramic body having alumina grains and grain boundary regions, and the method comprising at least the following steps: (a) beading the assembly to provide roughness The average value is less than 15 () one-inch thick chain degree of micro-inch; (b) immersing the component in a solution containing HF, HC1 and HN〇3 at a concentration of less than about 10% by volume. One or more; and
(c) 以雙絲熱喷塗製程於該組件之至少一部分上形成一鋁 塗層。 一種形成使用於製程處理室之一組件的方法,該組件至 少包含具有氧化鋁晶粒與晶界區域的陶瓷體,且該方法至少 包含下列步驟: (a) 珠擊該組件,以提供具有粗糙度平均值低於150微英 忖之一表面粗糙度; (b) 沈浸該組件於一溶液中,其中該溶液係包含濃度低於 7 1290341 約 2〇 體積百(diethylene glycol monobutyl ether)之一或多者;及 (c)以雙絲熱噴塗製程於該陶瓷體之至少一部分上形成一 鋁塗層。 【實施方式】 本發明之製程係製造用於一製程處理室中之具塗層組 件3 00,而該製程係具有提供增加組件3〇〇抗化學腐蝕之能 力,與抗塗層304自組件300上剝落之較佳能力。該製程可 用於形成在處理室36a中易受腐蝕影響之一或多個組件 300,其中該組件3〇〇諸如基板支撐件18之組件3〇〇。在一 實施例中,1料18(组件300係、包含使用於沉積處理室 36a中之沉積環15或覆蓋環17之一或多者。其他處理室組 件300之形式,舉例而言包含:處理室圍繞牆12之一部分, 如一側牆或屏蔽20、一襯墊(未示於圖中)、或頂板13 ;氣 體分散器39之_部分,如一氣體入口 33;氣體排放系統Μ 之一部分;與氣體激發器9G之—部分。第^圖為根據本發 明方法之實施例而形成之組件3〇〇的一實施例之戴面圖。 在一實施例中,處理室組件包含—陶㈣3〇2,該 陶瓷體3 02之表面先被處理,繼之再塗覆一 一 隻屬塗層。舉例 而言’根據本發明之製程,適於處理與塗霜 ^匕 立覆之陶瓷體302可 包括氧化鋁、碳化矽與氮化鋁之一或多者。 陶瓷體302被虛 理後係提供一表面306,而該表面306之特n〆 ^ 寺徵係允許陶兗體 302與上方塗層3〇4之間具有增強之鍵結 舉例而言,陶 1290341 ^^^^2之表面3〇6含有!處理的晶粒與晶界區域,而該處 理係藉^除表面 面306上提供一穩定的晶界區域,可使陶瓷體3〇2與上層塗 層304間形成適當強度之鍵結。相同地化學不純物或其他 鬆動的顆粒也可由陶兗體302之表面3〇6移除’藉此改善塗 層304在表面306上之黏著。 在一起始處理程序中,藉由珠擊陶瓷體3〇2之表面3〇6 來處理處理室組件300。珠擊可移除陶瓷體3 〇2之表面3〇6 上的任何不純物,並去除表面3 〇6上之任何鬆動或損傷的晶 粒,以提供一具有特定結構且粗糙的表面3〇6,進而增強塗 層304與表面306間的黏著力。在珠擊過程中,固體珠粒在 壓力下藉由空氣而推向表面3〇6,其中該壓力係足夠高以 使表面3 0 6粗糙化。該珠粒含有一材料,且該材料之硬度係 兩;陶瓷體302之硬度,以允許珠粒侵钱並粗輪化陶瓷體go] 之表面306,而形成粗糙與具特定結構之表面3〇6。合適的 珠粒材料係包含如氧化銘、玻璃、_土、或硬f塑膠。在一 實施例中’該珠粒包含砂狀氧化鋁,其中該氧化鋁具有適於 喷◊該表面之粒度(mesh size),諸如具有粒度^ 之砂 狀紹顆粒。珠擊可於如_個含有圍繞之外殼的珠擊處理室中 (未示於圖中)進行。 本案中發現改善表面3〇6處理之方法,係可以相對溫和 的珠擊製程清洗並處理該表面3〇6,而不過度粗糙化來加以 達成。該方法與傳統處理程序所預期的不相同,傳統程序一 般使用激進的珠擊製程,以高度粗糙化表面,進而增加任一 1290341 土I塗土上^^7。然而,在珠程期間二過量地粗糙化 表面,實際具塗層組 陶兗體302之表面306上形成微破裂與受損傷之晶界區域。 當該晶界層在陶瓷體302之表面顯著地被損傷時,則施加於 被損傷之表面306上的塗層304存在有較低之塗覆黏著力, 而陶瓷體302表面之晶粒以及結合於表面3〇6之塗層3〇4變 得鬆動,並導致塗層304分層或剝落。同樣地,施行珠擊期 間所產生的微破裂與受損傷的晶界層,在後續處理步驟中, 如濕式清洗步驟,受損情形將更為惡化。 故在此欲求維持珠擊的條件,以提供一較不激進的珠擊 製程並進而產生較低的表面粗糖度’其中表面粗糖度範圍 係如低於約150微英吋之粗糙度平均值(Ra),且又例如約由 60至140微英吋,甚至約低於12〇微英吋。表面3〇6之粗糙 度平均值係為沿著粗糙化表面3 〇 6之絕對偏移量的平均值, 其中該偏移係為該粗糙化特徵結構之頂端與凹處之平均線 的偏移。提供此表面粗糙度之合適的珠擊條件係包含:用於 推進珠粒朝向表面的空氣壓力範圍約由3〇 psi至約1〇〇 psi,甚至約由40 psi至約60 psi ;珠粒相對於表面的入射角 度範圍約由45度至90度,甚至約由75度至9〇度;珠粒由 珠擊室至該表面之行走距離約由4至12英吋,甚至為5至8 英忖。 可使用國際標準ANSI/ASME B.46.1 -1995來測量表面 3 06之性質,如粗糙度平均值,其詳細列出適當切除長度 (cut off length)與计鼻長度(eVaiuati〇n length)。下表 1 10 1290341 即為由所定義之粗糙度平均^^當切除長度值 最小與特有計^長度值:對應" ~- 表1 粗糙度平均值 切除長度 最小計算長度 特有計算長度 0至0.8微英吋 0.003英吋 0 · 0 1 6英叫· 0 · 0 1 6英口子 〇·8至4微英吋 0.010英叫· 0.050英吋 0.050英吋 4至80微英吋 0 · 0 3 0英对 0·160英口于 0·160英叫· 80至400微英时 0 · 1 0 0英叶 0.300英吋 0.500英吋 400微英吋及 0.300英吋 0.900英叫· 1.600英对 大於400微英吋 粗糙度平均值係以輪廓曲線儀(pr〇m〇m eter )或以掃描 式電子顯微鏡加以量測,其中輪廓曲線儀係在表面306上移 動一支針’以產生該表面306之粗糙情形的高度波動圖形, 而掃描式電子顯微鏡係使用一由該表面3〇6反射之電子束, 以產生該表面306之影像。 陶瓷體302之表面3〇6 一旦經珠擊處理後,表面3〇6可 進一步以第二處理步驟,如沈浸或浸洗,加以處理。處理溶 液包含一處理劑’該處理劑可去除表面3〇6上之不純物或清 洗表面306在珠擊期間所形成的鬆動晶粒,以製備能與塗層 3 04結合之表面306。表面3〇6之處理步驟係沈浸於該溶液 一段合適持續的時間以製備該表面3〇6,如約15秒至約30 分之期間’甚至約1 5秒至約1 5分。 經由處理溶液處理後,可發現非預期地產生塗層304與 1290341 良好的黏著力,竟ύ 液包含一足角低 濃度^溶液包含一足夠 此結果為非可預期 的處理劑,如IX導因於傳統製程常使用-較高漠度 製備表面3〇6而二::!積百分比之氫氟酸,以清洗與 面碎n n私 辰度的處理劑將更完善地清洗表 理= 然而,較佳係利用具有-足夠低漠度之處 理劑的處理溶液央:主 ^ 粒,而;^合、θ π 上任何殘餘物或弱鍵結晶 夕矣品埤也不曰形成或加劇組件300 之表面306上之微缺陷。 較於傳统以鉍- 低/辰度處理劑之處理溶液相 、較兩濃度之處理劑進行處理的製程,其因降低了 上因钕刻所造成晶界區域的損傷,故更加改善塗層 3〇4與陶瓷體3〇2間之鍵結。 實例中,陶瓷體302沈浸於含有適當低濃度之一酸 !生劑之g“生處理溶液中,其中該酸性劑包含氫氟酸(Bp )。 舉例^ ’該處理溶液可包含一主要含有HF的處理劑。氮 敗酸係提供表φ 3〇6之良好清洗,其並具有去除表面鳩上 之不純物與鬆動顆粒之能力,其中該顆粒係例如於珠擊或基 板1 6製程期間所形成之顆粒。氫氟酸也可以與累積在陶瓷 體302之表面3〇6上的不純物反應,並分解之,該不純物如 Si〇2、Ca〇或Mg〇。氫氟酸的適當低濃度係可為,如低於約 10體積百分比,士口約1至1〇體積百分比,甚至低於約5體 積百分比。 在另一實例中,陶瓷體302沈浸於一溶液中,該溶液含 有適當低濃度的一非氟化酸性處理劑。該非氟化酸性劑係提 12 1290341 供車乂低的處理而允許在降低表面306中微破 裂的成長與降低晶界區域之損傷的情形下,清洗與製備該表 面 S適的非氟化清洗劑包含如HC1或HN〇3。非氟化劑 合適的一低濃度係可約為低於2〇體積百分比,如濃度範圍 約由1至20體積百分比,甚至約低於丨〇體積百分比。在另 實例中,陶瓷體係沈浸於一驗性溶液中,如KOH溶液, 或一有機蝕刻劑溶液,如二乙二醇單丁(基)醚(diethylene glycol monobutyl ether)。 一將陶莞體3 0 2沈浸於溶液中而進行處理,則於陶竟 體3 02之至少一部分形成一金屬塗層3 〇4。在基板製程處理 室36a中,塗層3〇4含有可實質抗腐蝕之一或多種金屬,如 鋁、鈦、銅與鉻等其中之一或多種。金屬塗層3〇4之形成, 係用以保護陶瓷體302免於腐蝕,其中該塗層3〇4係可藉由 以下方法形成,如以處理室36a中之激發氣體加以形成,與 以一種提供金屬塗層304與陶瓷體302間強的鍵結之方法加 以形成。舉例來說,該塗層304係也可藉由一或多種化學或 物理沉積製程而加以塗覆,亦或可藉由火焰喷塗法或熱喷塗 法’如雙絲電弧喷塗(twin wire arc)方法、電漿弧嘴塗方法、 或氧燃料(oxy-fuel)氣體火焰喷塗。在製程處理室36&中, 適於降低腐蝕之金屬塗層304厚度,係約如至少〇 〇5 mm, 甚至低於約〇·5 mm之厚度。 在一實例中,金屬塗層係以一雙絲電弧熱喷塗製程而塗 覆至經處理之表面,其如2001年5月8曰頒證給Lazara等 人之美國專利第6,227,435 B1號與1997年12月9日頒證給 13 1290341(c) forming an aluminum coating on at least a portion of the assembly by a two-wire thermal spray process. A method of forming an assembly for use in a process chamber, the assembly comprising at least a ceramic body having alumina grains and grain boundary regions, and the method comprising at least the following steps: (a) beading the assembly to provide roughness a mean value of less than 150 micro-inch 表面 surface roughness; (b) immersing the component in a solution, wherein the solution comprises a concentration of less than 7 1290341 of about 2 diethylene glycol monobutyl ether or And (c) forming an aluminum coating on at least a portion of the ceramic body by a two-wire thermal spraying process. [Embodiment] The process of the present invention is to manufacture a coated component 300 in a process chamber, and the process has the ability to provide increased resistance to chemical corrosion of the component 3, and the anti-coating 304 from the component 300. The best ability to peel off. The process can be used to form one or more components 300 that are susceptible to corrosion in the processing chamber 36a, such as the components 3 of the substrate support 18. In one embodiment, a material 18 (component 300, comprising one or more of the deposition ring 15 or the cover ring 17 used in the deposition processing chamber 36a. The form of the other processing chamber assembly 300, for example, includes: The chamber surrounds a portion of the wall 12, such as a side wall or shield 20, a liner (not shown), or a top plate 13; a portion of the gas disperser 39, such as a gas inlet 33; a portion of the gas discharge system ;; Part of a gas energizer 9G. Figure 2 is a front view of an embodiment of an assembly 3 formed in accordance with an embodiment of the method of the present invention. In one embodiment, the processing chamber assembly comprises - (4) 3〇2 The surface of the ceramic body 302 is first treated, followed by a coating of a genus. For example, the ceramic body 302 suitable for processing and varnishing according to the process of the present invention may include One or more of alumina, tantalum carbide and aluminum nitride. The ceramic body 302 is imaginary to provide a surface 306, and the surface of the surface 306 is allowed to allow the ceramic body 302 and the upper coating 3 For example, in the case of an enhanced bond between 〇4, the table of pottery 1290341 ^^^^2 3〇6 contains the treated grain and grain boundary region, and the treatment provides a stable grain boundary region on the surface surface 306 to form a suitable strength between the ceramic body 3〇2 and the upper layer coating 304. Bonding. The same chemical impurities or other loose particles can also be removed from the surface 3〇6 of the ceramic body 302, thereby improving the adhesion of the coating 304 on the surface 306. Together with the process, by the bead shot The surface of the ceramic body 3〇2 is treated to process the chamber assembly 300. The bead strike removes any impurities on the surface 3〇6 of the ceramic body 3〇2 and removes any loose or damaged surface 336 The grains are provided to provide a surface having a specific structure and a rough surface 3〇6, thereby enhancing the adhesion between the coating 304 and the surface 306. During the beading process, the solid beads are pushed against the surface by air under pressure 3 〇6, wherein the pressure is sufficiently high to roughen the surface 306. The bead contains a material and the hardness of the material is two; the hardness of the ceramic body 302 to allow the beads to invade and coarsely round the ceramic Surface 306 of the body, forming a rough surface with a specific structure 3〇6 Suitable bead materials include, for example, oxidized, glass, _ soil, or hard f plastic. In one embodiment, the beads comprise sand-like alumina, wherein the alumina has a particle size suitable for sneezing the surface ( Mesh size), such as granules with a particle size of ^. The bead blast can be carried out in a bead blasting chamber (not shown) containing a surrounding outer casing. In this case, an improved surface 3 〇 6 treatment was found. In a method, the surface can be cleaned and treated with a relatively gentle bead blasting process without excessive roughening. This method is different from what is expected by conventional processing procedures, and conventional procedures generally use a radical beading process. The surface is highly roughened, and then any of the 1129034 soil I coated soil is added. However, during the bead pass, the surface is excessively roughened, and the surface 306 of the actual coated group of ceramics 302 forms a microfracture and damaged grain boundary region. When the grain boundary layer is significantly damaged on the surface of the ceramic body 302, the coating layer 304 applied to the damaged surface 306 has a lower coating adhesion, and the grain and bonding of the surface of the ceramic body 302. The coating 3〇4 on the surface 3〇6 becomes loose and causes the coating 304 to delaminate or peel off. Similarly, the microfracture and damaged grain boundary layer produced during the beading process will be worsened in subsequent processing steps, such as the wet cleaning step. Therefore, it is desirable to maintain the conditions of the bead strike to provide a less aggressive bead blasting process and thereby produce a lower surface roughness (where the surface roughness range is such as a roughness average below about 150 microinches). Ra), and again, for example, from about 60 to 140 micro-inch, or even less than about 12 micro-inch. The roughness average of the surface 3〇6 is the average of the absolute offsets along the roughened surface 3〇6, where the offset is the deviation of the average line of the top end and the recess of the roughened feature. . Suitable beading conditions for providing this surface roughness include: the air pressure for propelling the beads toward the surface ranges from about 3 psi to about 1 psi, even from about 40 psi to about 60 psi; the beads are relatively The angle of incidence at the surface ranges from about 45 to 90 degrees, and even from about 75 to 9 degrees; the distance from the bead chamber to the surface is from about 4 to 12 inches, or even from 5 to 8 inches. guess. The properties of surface 306, such as roughness averages, can be measured using the international standard ANSI/ASME B.46.1-1995, which details the appropriate cut off length and eVaiuati〇n length. Table 1 10 1290341 is the roughness average defined by ^^ when the cut length value is the smallest and the unique value ^ length value: corresponding " ~- Table 1 roughness average cut length minimum calculation length unique calculation length 0 to 0.8吋英吋0.003英吋0 · 0 1 6英叫· 0 · 0 1 6英口子〇·8 to 4 micro-inch 0.010 inches · 0.050 inches 0.050 inches 4 to 80 micro-inch 0 · 0 3 0 English to 0.160 inches at 0.160 inches · 80 to 400 micro-hours 0 · 1 0 0 inches 0.300 inches 0.500 inches 400 micro-inch and 0.300 inches 0.900 inches · 1.600 inches to more than 400 The micro-inch roughness average is measured by a profilometer (pr〇m〇m eter ) or by a scanning electron microscope, wherein the profilometer moves a needle ' on the surface 306 to create the surface 306 A highly undulating pattern of rough conditions, while a scanning electron microscope uses an electron beam reflected by the surface 3〇6 to produce an image of the surface 306. Surface 3〇6 of ceramic body 302, once subjected to bead blasting, surface 3〇6 may be further treated by a second processing step, such as immersion or dipping. The treatment solution contains a treatment agent which removes impurities on the surface 3〇6 or the loose grains formed by the cleaning surface 306 during the bead strike to prepare a surface 306 that can bond with the coating 304. The treatment step of surface 3〇6 is immersed in the solution for a suitable period of time to prepare the surface 3〇6, such as for a period of from about 15 seconds to about 30 minutes, even from about 15 seconds to about 15 minutes. After treatment with the treatment solution, it was found that the coating 304 had a good adhesion to 1290341, and the sputum contained a low angle solution containing a sufficient amount of the treatment agent which was unpredictable, such as IX. Conventional processes are often used - higher intensive preparation of surface 3〇6 and two::! The percentage of hydrofluoric acid will be better cleaned by the treatment agent for cleaning and surface nn. = However, it is better to use a treatment solution having a treatment with a sufficiently low degree of humidity: the main particle Any residue or weak bond crystallization on the θ π does not form or exacerbate micro defects on the surface 306 of the assembly 300. Compared with the conventional treatment process of the treatment solution phase of the 铋-low/min period treatment agent and the two-concentration treatment agent, the coating layer 3 is further improved because the damage of the grain boundary region caused by the engraving is reduced. The bond between 〇4 and the ceramic body 3〇2. In an example, the ceramic body 302 is immersed in a "raw treatment solution" containing a suitably low concentration of one acid; a green agent, wherein the acidic agent comprises hydrofluoric acid (Bp). Example ^ The treatment solution may comprise a primary HF The treatment agent. The nitrogen sulphuric acid system provides a good cleaning of the surface φ 3 〇 6 , which has the ability to remove impurities and loose particles on the surface ruthenium, wherein the granules are formed, for example, during the bead blasting or substrate 16 process. The hydrofluoric acid may also react with and decompose the impurities accumulated on the surface 3〇6 of the ceramic body 302, such as Si〇2, Ca〇 or Mg〇. The appropriate low concentration of hydrofluoric acid may be If less than about 10 volume percent, the mouth is about 1 to 1 volume percent, even less than about 5 volume percent. In another example, the ceramic body 302 is immersed in a solution containing a suitably low concentration of one. Non-fluorinated acidic treatment agent. The non-fluorinated acidic agent is 12 1290341 for the treatment of ruthenium to allow cleaning and preparation of the surface S in the case of reducing the growth of micro-cracks in the surface 306 and reducing the damage of the grain boundary region. Suitable The cleaning agent comprises, for example, HC1 or HN〇3. A suitable low concentration of the non-fluorinating agent may be less than about 2% by volume, such as a concentration ranging from about 1 to 20 volume percent, or even less than about 丨〇 volume percent. In another example, the ceramic system is immersed in an assay solution, such as a KOH solution, or an organic etchant solution, such as diethylene glycol monobutyl ether. 2 immersed in the solution for treatment, forming a metal coating 3 〇4 in at least a portion of the ceramic body 032. In the substrate processing chamber 36a, the coating 3 〇 4 contains one or more of substantial corrosion resistance a metal such as one or more of aluminum, titanium, copper and chromium, etc. The metal coating 3〇4 is formed to protect the ceramic body 302 from corrosion, wherein the coating 3〇4 can be obtained by the following method The formation is formed, for example, by the excitation gas in the processing chamber 36a, and is formed by a strong bonding between the metal coating 304 and the ceramic body 302. For example, the coating 304 can also be formed by a Or a variety of chemical or physical deposition processes For coating, or by flame spraying or thermal spraying, such as twin wire arc method, plasma arc nozzle coating method, or oxy-fuel gas flame spraying In the process chamber 36 &, the thickness of the metal coating 304 suitable for reducing corrosion is, for example, at least 〇〇5 mm, or even less than about 〇·5 mm. In one example, the metal coating system It is applied to the treated surface by a twin-wire arc thermal spraying process, as issued on May 8, 2001 to Lazara et al., US Patent No. 6,227,435 B1 and December 9, 1997. 1290341
Scruggs之美國專利第5,695,825號中所描述的,其中此兩項 專利係全部在此併入本案以作為參考。在雙絲電弧熱喷塗製 程中,一熱噴塗器(未示於圖中)包含兩個消耗性電極 (consumable electrode ),此兩消耗性電極被塑形並形成夾 角以使電弧在其間生成。舉例而言,消耗性電極包含塗覆至 表面3 0 6之金屬所形成的雙絲,而電極彼此間形成一角度以 在彼此最接近的點形成一放電。當於該消耗性電極間施加一 電壓,且一載氣在兩電極間流動時,兩消耗性電極間會產生 一電弧放電’其中載氣諸如空氣、氮氣或氬氣其中之一或多 者。電極間所產生之電弧會使電極上之金屬霧化與至少部分 液化,而由電弧電極所激發之載氣會使融化顆粒自熱喷塗器 推出’並朝向陶瓷體3 02之已處理表面306。該融化顆粒衝 撞陶瓷體302之表面306,並在該表面306上冷卻與凝結而 形成一塗層304。當雙絲變舊時,可將該些絲連續供入熱嘴 塗器中,以連續供應金屬材料。 在熱噴塗期間,選擇合適的操作參數以適當地調整塗覆 材料之特徵,該些參數係如當塗覆材料橫越由熱喷塗器至陶 瓷體表面306之路徑的溫度與速度。舉例而言,如氣體流逮、 率層級、粉末供應速率、載氣流速、熱噴塗器至該表面之 相隔距離(stan(j0ff distance )、與塗覆材料相對於表面3〇6 之沉積角度,這些參數係適以改善塗覆材料的塗佈,與塗層 304後續與表面3〇6間之黏著。舉例而言,消耗性電極之間 的電壓係經選擇而介於約丨〇伏特至約5 〇伏特,如約$ 〇伏 特^此外,消耗性電極之間流經的電流係可經選擇而介於約 14 1290341 ^^安培至約loop安培,如約3〇〇安培。電漿火炬(plasma torch)之功率層通常約由' ό至約 瓦。 相隔距離與沉積角度係經選擇,以調整表面上之塗覆材 料的沉積特性。舉例而言,相隔距離與沉積角度係經調整, 而可修改飛濺衝撞於表面306上之融化塗覆材料的圖案,以 形成如同『薄煎餅』與『薄板』之圖案。相隔距離與沉積角 度亦可經調整而修改塗覆材料衝撞表面306時的相、速度、 或液滴尺寸。在一實施例中,熱喷塗器與表面之間的相隔距 離約大於5英吋,而塗覆材料沉積於表面之角度約為9〇度。 對塗覆材料之速度加以調整,以適當地將塗覆材料沉積 於表面306上。在一實施例中,粉末狀塗覆材料之速度約由 100至3 00公尺/秒。另外,亦採用熱噴塗器,而使得當塗覆 材料衝撞表面306時之溫度至少為約熔化溫度。高於熔點的 溫度係可產生具有高密度與高鍵結強度的塗層。舉例而言, 在放電周圍之激發載氣的溫度可超過5〇 〇〇〇c。然而,在放電 周圍之激發載氣的溫度,也可設定為使塗覆材料在衝擊表面 3 06後之一段時間維持融化狀態之足夠低溫。舉例而言,一 段合適的時間至少約為數秒鐘。 根據本發明之製程加以處理與塗覆之一組件3〇〇,其係 可發現金屬塗層304與其下層陶瓷體3〇2間之鍵結實質地被 改善。舉例而言,在一濺鍍沉積處理室3 6 a中,根據本發明 之製程而加以處理與塗覆後之組件3 〇 〇,其效能為之增進, 其中於處理室36a中形成之濺鍵材料可累積在組件3〇〇之暴 1290341 露表面308上至少約〇.2mm,甚^高達imm,甚或高達i.5mm 之厚度,而實質不 在一實例中,上方所描述之處理與塗覆製程,係可製造 用於處理室36a中具塗層之組件3〇〇。舉例而言,為了製造 組件300,陶瓷體302係可以陶瓷粉末與一黏結劑之混合物 加以製備’其中該黏結劑可為一有機黏結材料。在一模具 中,陶瓷粉末與黏結劑例如藉由鑄漿成型法(slip casting ) 而被塑形成為一合適的陶瓷體預塑物(pref〇rm ),或藉由猛 力加壓、均衡加壓,或帶鑄成型法(tapecasting)而形成。 舉例而言,在一實例中,陶瓷粉末與黏結劑被塑形成為使用 於沉積處理室36a中的一沉積環或覆蓋環之形式。之後,燒 結此成型之預塑物,以使得包含陶瓷體3〇2之陶瓷材料變 硬。合適的連接器或其他結構,係可在燒結前形成於成型之 預塑物内。已燒結陶瓷體302也可依照欲求厚度而研磨形 成,而其他結構也可鑽入或以機械加工而製造於多孔性陶瓷 材料中。一旦陶瓷體302形成欲求之形狀,上述處理製程, 係可藉由珠擊與沉浸於一溶液中加以處理陶瓷體3〇2之表 面,以製備用於與金屬塗層3〇4連結之陶甍體3〇2表面3〇6 而。繼之,金屬塗層304以熱噴塗一金屬材料至表面3〇6上 而形成。 在另一實例中,係執行處理與塗覆製程以再磨光已用於 基材裝程處理至36a中之組件3〇〇,例如,對於處理室36& 中暴露於激發氣體之受損組件3〇〇,施以再磨光步驟。在此 實例中’組件300包含陶瓷n 3〇2與受損金屬塗層3〇4,其 16 1290341 由去除金屬塗層304,與處理並塗覆其下層之表面3〇6, 而可使組件300加以再磨[與 舉例而言,係藉由如上述之珠擊製程,或藉由另一金屬去除 方法,如蝕刻製程,而加以去除。該金屬塗層3〇4 — 於土 fijsL "is 除後,其下層表面306係根據本發明製程,以珠擊並沉浸於 一處理溶液中。最後,表面306再次如藉由熱塗佈製程而以 金屬塗層302塗覆之。 第2圖係為說明根據本發明所揭示之處理與塗覆製程之 一流程圖。如流程圖所示,該製程一般包含下列步驟:(〖)珠 擊一組件300,以提供具有粗糙度平均值小於約丨5〇微英对 之表面粗糙度;(ii)沈浸陶瓷體於一溶液中,該溶液具有足 夠低的濃度,以降低陶瓷體之晶界區域之蝕刻;及(iii)形成 一金屬塗層,該塗層係塗覆於陶瓷體之至少一部分上。 已處理與具塗層之組件300可使用於製程處理室36a 中,其中如第3圖所示,處理室3 6a係為多重處理室平台1〇0 之部分。多重處理室平台100,舉例而言,係可為Applied Materials,Santa Clara,California 所提供之商業使用的 『ENDURA』系統。在此所顯示之平台100的特定實施例, 係適用於製造一平面矽晶圓基板16,而其僅用於說明本發 明,但不應限制本發明之範圍。多重處理室平台1 〇〇,一般 包含:互相連結之處理室36a-d、114、1〇2、118的群集 (cluster );與一包含機械臂裝置132之基板傳輸件,其係用 以在處理室36 a-d、114、102、118間傳送基板16。機械臂 裝置132包含具有葉片134之機械臂,該葉片134係用以支 17 1290341 板16^加載鎖定^^12()、122係接收包含有 ° 一 氣處理室~177^'^~^ 定位基板16以預備進入製程程序,並去除基板16中之氣 體,以除去基板16之〉可染物,避免該污染物破壞製程處理 室36a-d之高真空環境。一預清洗處理室U4係在任一沉積 步驟刖,用於清洗基板1 6,而一冷卻處理室丨〇2係用於冷卻 基板16。一製程程序裝置136係用以控制機械臂裝置132, 如下指令執行一程序,使機械臂裝置132在各處理室36a_d、 ii4、i〇2、118間傳送基板16。一般而言,製程程序裝置136 係控制機械臂裝置132,將基板16自加載鎖定處理室12〇、 122之一者中取出,再傳送至定位與除氣處理室us中,繼 之再依序傳送至預清洗處理室114與製程處理室36a_d之一 或多者中’完成之後再傳送至冷卻處理室1〇2中。 如第4圖所示,多重處理室平台1〇〇至少具有一 pvD 處理室36a,其係用以在基板16上濺鍍沉積一層,其中該層 如鈕、氮化钽或銅其中之一或多者。在PVD處理室36&中, 基板支撐件18係用以支撐基板16。基板16經由一位於處理 室3 6a之側牆45中的基板載入口 (未示於圖中)而導入處 理室36a,並被放置在支撐件18上。在傳送基板丨6進出處 理室36a期間,支撐件18係藉由支撐件升降波紋管(未示 於圖中)加以上升或下降,及一升降指狀物組件(亦未示於 圖中)係用於將基板16升高與下降,以使基板16放置在支 撐件1 8上。 支撐件1 8包含一或多個環,係用以至少覆蓋支撐件】8 18 1290341 件錢,其中該 環諸如沉積環__& 環1 7係覆蓋位於支撐件! 8上靜 儿% 15與覆盖 一 S上之靜電吸座的至少一部分(未 ::),以降低靜電吸座在處理冑…中暴露於激發氣 ”降低顆粒沉積在靜電吸座上之機率。在一實例中,沉 積% 15至少部分圍繞基板16,以保護支料^ 8不被基板 16所覆蓋之部分。覆蓋環17至少圍繞沉積環15之-部分, 並協助降低顆粒沉積於沉積環15與其下層支料Η兩者之 上。根據本發明之一態樣,沉積環15與覆蓋冑Η係可根據 本發明製程加以處理與塗覆。根據本製程所提供具強鍵結之 金屬塗層304,係使沉積環15、覆蓋環17在無過量熱膨服 應力或塗層304之分層情形下,容納更大量之沉積物。因此, 根據本製程而處理與塗覆之沉積環15與覆蓋環17,係可增 強其抗腐蝕性,並對於其下層之基板支撐件18,提供較佳抗 腐蝕保護。 一藏鑛氣體供應器23將錢鍍氣體導入處理室中, 以使藏鑛氣體在一製程區中維持於次大氣壓力(sub atmospheric pressure )下。濺鍍氣體經由一氣體入口 33導入 處理室36a中’其中該氣體入口 33經由氣體輸入25a、25b, 而各自連接至一或多個氣體源24、27。一或多個質流控制器 26係用以控制個別氣體的流量,而個別氣體在導入處理室 36a前,可先在混合岐管31中預先混合,或也可各自獨立導 入處理室36a内。濺鍍氣體一般包含非反應性氣體,如氬氣 或氣氣’當該氣體被激發成一電聚時,其會具能量地撞擊及 19 1290341 组、或氮化鈕等濺 14,並自乾材"濺鍍出如銅 瑕何科。濺鍍氣體也包含一及一~7Γ~-- 反應性氣體,如氮氣。相同地, 熟習此技術者係可理解,I你、拖μ ^ ώ 其他錢錄氣體之組成也包含其他反 應性氣體或其他形式之非反應性氣體。 八 一排放系統2 8係批制_饰& 丄 矛徑制處理室36a中濺鍍氣體之壓力, 並排放處理室36a内過孴的盔脚如 士止γ 1的氣體與副產物氣體。在處理室36a 中,排放系統28包含一媸名^ 、 排軋口 29,該排氣口 29連接於通向 一或多個排氣幫浦之排翁瞢 哪虱吕線34 〇在排氣管線34中且有一 節流間37’其係用以控制處理室%中之料氣體心。在 處理室…中’滅鍍氣體之壓力—般設定在次大氣壓力之程 度,如約2至1〇 mT〇rr (亳托) PVD處理至36a更包含—濺錢乾材14,其中該乾材μ 包3鈦並面向基板16。一準 準直儀(未不於圖中)係可按需求 架汉在數材14與基板支撐件 牙彳干之間。PVD處理室36a也可 具有屏蔽20,以保護處理室 α Α 至“a之牆12免受濺鍍材料攻擊, 且一般來說,該屏蔽η 亦可作為陽極接地平面。屏蔽 為電性浮接或接地。靶材14 由蒋蔽20係 材4與處理室3“係為電性絕緣, 且其係連接至一電壓源, 原 不過該電壓源可 為其他形式,如RF電 电源在一實例中,DC電源22、靶鉍Scruggs is described in U.S. Patent No. 5,695,825, the entire disclosure of which is incorporated herein by reference. In a twin wire arc thermal spray process, a thermal sprayer (not shown) contains two consumable electrodes that are shaped and angled to create an arc therebetween. For example, the consumable electrode comprises a double filament formed by a metal coated to the surface 306, and the electrodes form an angle with each other to form a discharge at a point closest to each other. When a voltage is applied between the consumable electrodes and a carrier gas flows between the electrodes, an arc discharge is generated between the two consumable electrodes, wherein one or more of the carrier gases such as air, nitrogen or argon. The arc generated between the electrodes will atomize and at least partially liquefy the metal on the electrode, and the carrier gas excited by the arc electrode will cause the melted particles to push out of the thermal sprayer' and toward the treated surface 306 of the ceramic body 302. . The melted particles impinge on the surface 306 of the ceramic body 302 and are cooled and condensed on the surface 306 to form a coating 304. When the twin filaments become old, the filaments can be continuously supplied into the nozzle applicator to continuously supply the metal material. During thermal spraying, suitable operating parameters are selected to properly tailor the characteristics of the coating material, such as when the coating material traverses the temperature and velocity of the path from the thermal sprayer to the ceramic body surface 306. For example, such as gas flow rate, rate level, powder supply rate, carrier gas flow rate, distance between the thermal sprayer and the surface (stan (j0ff distance), and deposition angle of the coating material relative to the surface 3〇6, These parameters are suitable to improve the coating of the coating material and the subsequent adhesion of the coating 304 to the surface 3 〇 6. For example, the voltage between the consumable electrodes is selected to be between about 丨〇 volt to about 5 volts, such as about $ volts ^ In addition, the current flowing between the consumable electrodes can be selected to be between about 14 1290341 ^ ^ amps to about loop amps, such as about 3 amps. Plasma torch ( The power layer of the plasma torch is usually from about ό to about 瓦. The separation distance and the deposition angle are selected to adjust the deposition characteristics of the coating material on the surface. For example, the separation distance and the deposition angle are adjusted, and The pattern of the melted coating material splashed against the surface 306 can be modified to form a pattern like "pancake" and "thin plate." The distance and deposition angle can also be adjusted to modify the phase of the coating material impact surface 306. , Degree, or droplet size. In one embodiment, the distance between the thermal sprayer and the surface is greater than about 5 inches, and the coating material is deposited at the surface at an angle of about 9 degrees. The speed is adjusted to properly deposit the coating material on the surface 306. In one embodiment, the powder coating material is at a speed of from about 100 to about 300 meters per second. In addition, a thermal sprayer is also employed. The temperature at which the coating material impacts the surface 306 is at least about the melting temperature. Temperatures above the melting point produce a coating having a high density and high bonding strength. For example, the temperature of the excited carrier gas around the discharge. It may exceed 5 〇〇〇〇 c. However, the temperature of the excited carrier gas around the discharge may also be set such that the coating material maintains a sufficiently low temperature of the melted state for a period of time after the impact surface 306. For example, a section A suitable time is at least about several seconds. One of the components 3 is treated and coated according to the process of the present invention, which is found to substantially improve the bonding between the metal coating 304 and its underlying ceramic body 3〇2. In terms of In a sputtering deposition processing chamber 3 6 a, the processed and coated component 3 根据 according to the process of the present invention has an improved performance, wherein the splash-bonding material formed in the processing chamber 36a can accumulate in The assembly 3 129 129 129 129 034 129 129 129 129 129 129 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 308 For use in the coated assembly 36a of the chamber 36a. For example, to fabricate the assembly 300, the ceramic body 302 can be prepared from a mixture of ceramic powder and a binder, wherein the binder can be an organic bonding material. In a mold, the ceramic powder and the binder are molded into a suitable ceramic body preform (pref〇rm) by, for example, slip casting, or by violent pressurization and equalization. Pressurized, or formed by tapecasting. For example, in one example, the ceramic powder and binder are shaped to be in the form of a deposition ring or cover ring for use in deposition processing chamber 36a. Thereafter, the molded preform is sintered to harden the ceramic material containing the ceramic body 3〇2. Suitable connectors or other structures can be formed into the formed preform prior to sintering. The sintered ceramic body 302 can also be formed by grinding according to the desired thickness, and other structures can be drilled or machined into the porous ceramic material. Once the ceramic body 302 is formed into a desired shape, the above treatment process can be performed by treating the surface of the ceramic body 3〇2 by bead blasting and immersing in a solution to prepare a ceramic enamel for bonding with the metal coating 3〇4. The surface of the body 3〇2 is 3〇6. Next, the metal coating 304 is formed by thermally spraying a metal material onto the surface 3〇6. In another example, a processing and coating process is performed to re-polish the components 3 that have been used in the substrate processing to 36a, for example, for damaged components exposed to the excitation gas in the processing chamber 36 & 3〇〇, apply the re-polishing step. In this example, the assembly 300 comprises a ceramic n 3〇2 and a damaged metal coating 3〇4, the 16 1290341 is removed from the metal coating 304, and the surface 3〇6 of the lower layer is treated and coated to allow assembly 300 is reground (for example, by a beading process as described above, or by another metal removal process, such as an etching process). The metal coating 3〇4 — after the soil fijsL "is is removed, the lower surface 306 is subjected to a process according to the invention, which is beaded and immersed in a treatment solution. Finally, surface 306 is again coated with metal coating 302 as by a thermal coating process. Figure 2 is a flow chart illustrating the processing and coating process disclosed in accordance with the present invention. As shown in the flow chart, the process generally comprises the steps of: (b) beating a component 300 to provide a surface roughness having an average roughness of less than about 5 〇 〇; (ii) immersing the ceramic body in a In solution, the solution has a concentration low enough to reduce etching of the grain boundary regions of the ceramic body; and (iii) forming a metal coating applied to at least a portion of the ceramic body. The treated and coated assembly 300 can be used in the process chamber 36a, wherein as shown in Fig. 3, the process chamber 36a is part of the multiple process chamber platform 1〇0. The multi-chamber platform 100, for example, is a commercially available "ENDURA" system available from Applied Materials, Santa Clara, California. The particular embodiment of the platform 100 shown herein is suitable for use in the fabrication of a planar germanium wafer substrate 16, which is merely illustrative of the invention, but should not limit the scope of the invention. The multiple processing chamber platform 1 generally includes: a cluster of interconnected processing chambers 36a-d, 114, 1 2, 118; and a substrate transport member including a robotic arm assembly 132 for The substrate 16 is transferred between the processing chambers 36 ad, 114, 102, and 118. The robot arm device 132 includes a mechanical arm having a blade 134 for supporting a 17 1290341 plate 16 ^ loading lock ^ ^ 12 (), 122 system receiving includes a gas processing chamber ~ 177 ^ ' ^ ~ ^ positioning substrate 16 is pre-programmed into the process and the gas in the substrate 16 is removed to remove the > dyeable material of the substrate 16 from the high vacuum environment of the process chambers 36a-d. A pre-cleaning chamber U4 is used to clean the substrate 16 in any deposition step, and a cooling chamber 丨〇 2 is used to cool the substrate 16. A process program device 136 is used to control the robot arm device 132. The following command executes a program to cause the robot arm device 132 to transport the substrate 16 between the process chambers 36a-d, ii4, i2, and 118. In general, the process program device 136 controls the robot arm device 132 to take out the substrate 16 from one of the load lock processing chambers 12, 122, and then transfer it to the positioning and degassing processing chamber us, and then sequentially The transfer to the one of the pre-cleaning process chamber 114 and the process chambers 36a-d is completed and then transferred to the cooling process chamber 1〇2. As shown in FIG. 4, the multiple processing chamber platform 1A has at least one pvD processing chamber 36a for sputtering a layer on the substrate 16, wherein the layer is one of a button, a tantalum nitride or a copper. More. In the PVD processing chamber 36 &, the substrate support 18 is used to support the substrate 16. The substrate 16 is introduced into the processing chamber 36a via a substrate loading port (not shown) in the side wall 45 of the processing chamber 36a, and is placed on the support member 18. During the transfer of the substrate 丨6 into and out of the processing chamber 36a, the support member 18 is raised or lowered by a support lifting bellows (not shown) and a lifting finger assembly (also not shown). It is used to raise and lower the substrate 16 to place the substrate 16 on the support 18. The support member 18 includes one or more rings for covering at least the support member 8 18 1290341 pieces of money, wherein the ring such as the deposition ring __& the ring 17 is covered by the support member! 8 上静儿% 15 and covering at least a portion of the electrostatic chuck on the S (not::) to reduce the exposure of the electrostatic chuck to the excitation gas in the treatment ” ... reduces the probability of particles depositing on the electrostatic chuck. In one example, the deposition % 15 at least partially surrounds the substrate 16 to protect portions of the support 8 that are not covered by the substrate 16. The cover ring 17 surrounds at least a portion of the deposition ring 15 and assists in reducing particle deposition on the deposition ring 15 In addition to the underlying support, in accordance with one aspect of the present invention, the deposition ring 15 and the cover tether can be treated and coated in accordance with the process of the present invention. A metal bond with a strong bond is provided in accordance with the present process. 304, the deposition ring 15 and the cover ring 17 are accommodated in a larger amount of deposits without excessive thermal expansion stress or delamination of the coating 304. Therefore, the deposition ring 15 treated and coated according to the present process is The cover ring 17 can enhance its corrosion resistance and provide better corrosion protection for the lower substrate support 18. A mine gas supply 23 introduces a gas plating gas into the processing chamber to make the gas Maintained in a process area Under sub atmospheric pressure, the sputtering gas is introduced into the processing chamber 36a via a gas inlet 33, wherein the gas inlets 33 are each connected to one or more gas sources 24, 27 via gas inputs 25a, 25b. One or more mass flow controllers 26 are used to control the flow rate of the individual gases, and the individual gases may be pre-mixed in the mixing manifold 31 before being introduced into the processing chamber 36a, or may be separately introduced into the processing chamber 36a. The sputtering gas generally contains a non-reactive gas, such as argon or gas. When the gas is excited to form an electropolymer, it will energetically collide with the 19 1290341 group, or the nitride button, etc. "sputtering out such as copper enamel. Sputtering gas also contains one and one ~7 Γ~-- reactive gas, such as nitrogen. Similarly, those skilled in the art can understand, I, drag μ ^ ώ other The composition of the money recording gas also contains other reactive gases or other forms of non-reactive gas. Bayi Emissions System 2 8 Series _ Decoration & 丄 丄 制 处理 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 36 The helmet feet in the room 36a Gas and by-product gas of γ 1. In the processing chamber 36a, the discharge system 28 includes a nickname, a venting port 29, which is connected to a row leading to one or more exhaust pumps.翁瞢瞢虱吕线34 〇 is in the exhaust line 34 and has a flow 37' which is used to control the gas core in the processing chamber. In the processing chamber, the pressure of the deplating gas is generally set at The degree of subatmospheric pressure, such as about 2 to 1 〇 mT 〇rr (亳托) PVD treatment to 36a, further includes - splashing dry material 14, wherein the dry material is coated with 3 titanium and faces the substrate 16. A quasi-collimator (not in the figure) can be placed between the number 14 and the substrate support gingival on demand. The PVD processing chamber 36a may also have a shield 20 to protect the process chambers α Α to "a wall 12 from attack by sputtering materials, and in general, the shield η may also serve as an anode ground plane. The shield is electrically floating. Or grounding. The target 14 is electrically insulated from the processing chamber 3 by the Shield 20, and is connected to a voltage source, but the voltage source can be in other forms, such as an RF power supply in an example. Medium, DC power supply 22, target
14、與屏蔽20視為一氣體激狢哭办 H 巩體激發窃90來操作,該激發器9f) 係能激發⑽氣體成為電漿,以錢材料。加電源η。 對於屏蔽20而施加一 DC雷壓f如· Dr啻广 、 相 電壓(如· DC電壓脈衝)至乾 14。在處理室36a中,施加電壓於濺鍍靶材η以產生 U琢係可激發滅鑛t體,以形成可自乾材i4 $賤鑛材料之 20 1290341 電漿。經由電漿自靶材濺鍍出的材料,係沉積於基板丨6上, 其並能與電聚之氣體組成產生反應,而在基板16上形成一 沉積層。 處理室36a更包含一具有磁場產生器35之磁控管32, 該磁場產生器35可在接近處理室36a之乾材14處產生磁場 105,以增加鄰近於靶材14之高密度電漿區域38内之離子 雄、度域係’用以改善乾材材料之錢鑛。此外,可使用一改良 之磁控管32而允許銅的維持性自身濺鍍(sustained self-sputtering )’或紹、鈦、或其他金屬材料的濺鑛,且可 同時減少用於轟擊靶材之非反應性氣體之需求,此例子係如 同頒證給Fu,且專利名稱為『旋轉濺鍍磁控管组件』之美國 專利第6,183,614號,與頒證給Gopairaja等人,且專利名稱 為『用於填充銅介層孔之整合製程』之美國專利號碼第 6,2 74,008號中所描述,此兩文在此係全部併入本案以作為參 考。磁場105係延伸通過實質非磁性之靶材14,而進入真空 處理室36a中。在一實例中,磁控管32在靶材14上產生一 半超環面(semi-toroidal)磁場。在一實施例中,磁控管32 由幾近把材14之中心點,水平延伸至靶材14可用區域之邊 緣。在一實例中,磁控管32包含用以使磁控管32環繞旋轉 軸78而旋轉之一馬達1〇6。馬達1〇6 一般藉由軸IQ*而裴設 至磁控管32之磁性軛鐵98上,其中麵1〇4係沿著旋轉軸78 延伸。 本發明之PVD製程係使用一電腦程式產品i4i加以執 行’該電腦程式產口口。141包含製程程序裝置136,並於控制 21 1290341 5圖所示,f中該控制器30係包含—遠 接於具有周元件之體系中 (CPU) ’ 例如 Synergy Microsystems,Calif〇rnia 所製造商業 上可得的684〇0微處理器。此電腦程式碼係可使用任何傳統 之電腦可讀程式語言加以撰寫,如組合語言、c、c + +、^ Pascal。合適的程式碼係使用傳統文書編輯器輸入於單—= 案或複數個槽案中’並储存或内建於—電腦可使用媒體,: 電腦的記憶體系統。若輸入之程式碼文字為一高階語言則 此程式碼會被編#,且此編譯後之程式瑪,繼之會連結至預 先編譯視窗函式庫常式的目的碼。為了執行被連結的編零目 的碼’系統使用者需執行該目的碼,以致使電腦系統將該纽 言载入記憶體中,CPU再自記憶體讀取與實行該程式碼,: 完成程式中所定義之任務。 使用者將-製程設定與製程處理室號碼輸入至一製程 選擇器程式碼142中。該製鋥兮宏在达 中進〇… 為用於特定製程處理室 進仃特疋程序之數組製程參數, 石民制< ▲ & 肝再辨識為預定設定號 馬。製程參數係關於製程條件,該製 Μ碘象I程條件如製程氣體組成 一流率、▲度、壓力、氣體激發製 DC Φ ^ ^ ^ 径怿件(如非脈衝或具脈 衡之DC電源層級與磁場 處理室牆之溫度。 羊“及)、冷部氣體覆力、與 製私程序裝置130包含··用以接受來 m 149 ^ ^ 丧又來自製程選擇器程式14. The shield 20 is regarded as a gas-exciting crying H. The scaffold is activated to steal 90, and the exciter 9f) can excite (10) the gas into a plasma to the money material. Add power η. For the shield 20, a DC lightning pressure f, such as Dr., and a phase voltage (e.g., DC voltage pulse), are applied to the dry conductor 14. In the process chamber 36a, a voltage is applied to the sputter target η to produce a U-system that excites the quenched t body to form a 20 1290341 plasma that is self-drying material i4 $贱 mineral material. The material sputtered from the target via the plasma is deposited on the substrate 丨6, which reacts with the electropolymerized gas composition to form a deposited layer on the substrate 16. The processing chamber 36a further includes a magnetron 32 having a magnetic field generator 35 that generates a magnetic field 105 near the dry material 14 of the processing chamber 36a to increase the high density plasma region adjacent to the target 14. The ion male and the genus in 38 are used to improve the money mine of dry materials. In addition, a modified magnetron 32 can be used to allow for sustained self-sputtering of copper or splashing of titanium, titanium, or other metallic materials, and can simultaneously reduce the use of bombardment targets. The demand for a non-reactive gas is the same as that granted to Fu, and the patent name is "Rotating Sputtered Magnetron Assembly", US Patent No. 6,183,614, and issued to Gopairaja et al. The U.S. Patent No. 6,2,74,008, the entire disclosure of which is incorporated herein by reference. The magnetic field 105 extends through the substantially non-magnetic target 14 into the vacuum processing chamber 36a. In one example, magnetron 32 produces a semi-toroidal magnetic field on target 14. In one embodiment, the magnetron 32 extends horizontally from the center point of the adjacent material 14 to the edge of the available area of the target 14. In one example, magnetron 32 includes a motor 1〇6 for rotating magnetron 32 around rotating shaft 78. The motor 1〇6 is typically applied to the magnetic yoke 98 of the magnetron 32 by the shaft IQ*, wherein the face 1〇4 extends along the axis of rotation 78. The PVD process of the present invention uses a computer program product i4i to execute the computer program. 141 includes a process program device 136, and is shown in the control 21 1290341 5, where the controller 30 includes - in a system with a peripheral component (CPU) 'for example, commercially available from Synergy Microsystems, Calif〇rnia Available 684〇0 microprocessor. This computer code can be written in any traditional computer readable programming language, such as a combination language, c, c++, ^ Pascal. The appropriate code is entered in a single-- or multiple-slot case using a traditional paper editor and stored or built-in. The computer can use the media: the computer's memory system. If the input code text is a higher-level language, the code will be edited #, and the compiled program will be linked to the object code of the pre-compiled window library routine. In order to execute the linked zero-coded code, the system user needs to execute the object code so that the computer system loads the message into the memory, and the CPU reads and executes the code from the memory: The task defined. The user enters the process settings and the process chamber number into a process selector code 142. The system is used to process the array process parameters for the special process chamber. The Shimin system < ▲ & liver re-identification is the predetermined setting number. The process parameters are related to the process conditions. The I-process conditions of the iodine image such as process gas composition first-rate rate, ▲ degree, pressure, gas excitation system DC Φ ^ ^ ^ diameter element (such as non-pulse or DC power supply level with pulse balance) And the temperature of the magnetic field treatment chamber wall. The sheep "and", the cold part of the gas, and the private program device 130 contain ··· accepting m 149 ^ ^ mourning and from the process selector program
、、 的已辨識之製程處理室36及數細制$ A 碼·祐田认〜& 及數組製程參數的程式 碼,並用於控制各個製程處理室36& 可輪入盤袖制^ 之刼作。數個使用者 ,數個製程設定號碼與製程處理室 至5虎碼,或一個使用者 22 1290341 _可輸入多個1程設定號^與製程岸 一 序裝置 以致使製^ 置1 36更佳地包含一程κ 所選擇之製程。製程程序絮 工、>&馬,以會 室36a-d之操作,以判定處理室現下列步驟··⑴監控處g 決定在處理室36a-d進行何種製6玨d疋否正為使用中,⑴ 該欲求製程係基於特定製程呈;及丄出)執行欲求製程, 的可利用性。亦可採用傳统致 與欲進行之製程種類 輪詢…Uing)。當排定待二:之處理室36“之方法’例如: 係設計為可考量所使用之數程程二,製程程序裝… 所選擇裳程之欲求製程條件兩者條件之差:現於 件與鍵入需求之每一特定广之差“考1現存條 式設計師欲求含括以決定年紀』,或與-系統程 要特徵之„。 先彳何其他重 :旦製程程序裝置136決定接續使用之製程處理室與製 至一 Ή職㈣送特U程指設定參數 i官理者程式碼14",以執行該製程設定,苴中 ^式碼144係根據程序裝置136所決定的製程設定,加以抑 :製程處理室36“中之多個製程任務。舉例而言,: j至S理者程式石馬144係包含用於控制在所描述之製程處理 至36a中的PVD製程操作之程式碼。處理室管理者程式石馬 14斗亦控制各個處理室組件之程式碼或程式碼模組之執行, 而该些程式碼係控制用於進行所選擇之製程設定之處理室 件300的操作。處理室組件程式碼之實例係為··一基板定 弋馬1 4 5、氣流控制程式碼】4 6、排放控制程式碼^ * 7、 23 1290341 器控制程式碼1 48、與電壓源控制程式碼1 49。對於熟 ~~ —___ ___ ________ _ _ 習本技術者可明瞭,依據製程處理室36a之欲執行之製程, 亦可包含其他處理室控制程式碼。 在操作中,處理室管理者程式碼1 44係根據所執行之特 定製程設定而選擇性排定或傳唤製程組件程式碼。處理室管 理者程式碼1 44排定製程組件程式碼之方式,係相似於程序 裝置程式碼排定接續執行之處理室36a-d與製程設定之方 式。處理室管理者程式碼丨44 一般包含之步驟係有:監控各, and the identified process chamber 36 and the number of fine code A code · You Tian recognized ~ & and array process parameters, and used to control each process chamber 36 & Work. Several users, several process setting numbers and process processing rooms to 5 tiger codes, or one user 22 1290341 _ can input multiple 1-way setting numbers ^ and process bank first-order devices to make the system 1 36 better The ground contains a process selected by κ. The process program, >& horse, operates in the chambers 36a-d to determine the processing chamber. The following steps are performed. (1) The monitoring station g determines which system is to be processed in the processing chambers 36a-d. In use, (1) the desired process is based on a specific process; and the execution of the desired process is performed. It is also possible to use the traditional type of process to be polled... Uing). When the process room 36 is scheduled to be "processed", for example: the system is designed to take into account the number of processes used, the process program is loaded... The difference between the conditions of the desired process conditions: the current condition Each of the specific differences between the type and the demanding requirements is as follows: "1 is the current designer, and the system is required to determine the age," or - the system is required to be characterized. What is the other weight: the process program device 136 decides to continue to use The process processing room and the system to the fourth job (four) to send the special U program refers to setting the parameter i official program code 14 " to execute the process setting, the system code 144 is determined according to the process setting determined by the program device 136, Suppress: a plurality of process tasks in the process chamber 36. For example, the j to S program program 144 includes a code for controlling the PVD process operation in the described process process to 36a. The process room manager program Shima 14 also controls the execution of code or code modules of the various process room components that control the operation of the process chamber 300 for performing the selected process settings. The example of the processing room component code is: · a substrate fixed 1 1 4 5, air flow control code] 4 6, emission control code ^ * 7, 23 1290341 control code 1 48, and voltage source control program Code 1 49. For those skilled in the art, it will be apparent to those skilled in the art that, depending on the process to be executed by the process chamber 36a, other process control code codes may be included. In operation, the process room manager code 1 44 selectively schedules or calls the process component code based on the custom program settings being executed. The processing room manager code 1 44 sets the custom component code, which is similar to the processing device code to execute the processing chambers 36a-d and process settings. The processing room manager code 丨44 generally includes the following steps: monitoring each
個處理室組件300;基於欲被執行的製程設定之製程參數來 決定需被操作之組件3 00 ;以及執行相應於監控與決定步驟 之處理室組件程式碼。 現將加以描述特定處理室組件程式碼之操作。基板定位 程式碼145包含用於控制處理室組件3〇〇之程式碼,其中該 組件300係被用於傳送一基板16至基板支撐件18上,並且 可選擇地在處理室3 6中將基板1 6升舉至欲求高度,以控制 基板16與靶材間之間距。當基板16被傳送至處理室中 時,基板支撐件18係降低以接收基板16,而後,支撐件Η 在處理室36a中上升至欲求高度。基板定位程式碼145係相 應於來自處理室管理者程式語碼44之關於支撐件高度的製 程設定參數,而控制支撐件18之位移。 氣流程式碼146係用於控制製程組成與流率。一般用於 每-製程氣趙之氣體導管34,係包含安全關閉閥(未示於圖 中),其可自動或手動關閉進入處理室36a之製程氣體流量。 當在製程中使用毒性氣體時,—此亡&相^ 24 1290341 定位於每一氣體導管3 4上。氣流程式碼1 4 6係控制安全關 閉閾之開/關狀態,並使質流控制器加/減速以 流速率。氣流程式碼1 46如同所有處理室組件程式碼,係藉 由處理室管理者程式碼144加以執行,並由處理室管理者程 式码14 4接收關於欲求氣體流率之製程參數。氣流程式碼1 4 6 之操作,一般係藉由重複讀取必須的質流控制器、比較讀取 值與接收至管理者程式碼144之欲求流率兩者之差異、再依 需要情況加以調整流率。此外,氣流程式碼1 4 6包含步驟如 下··監控不安全之氣流流率,並當監測到不安全狀況產生 時’啟動安全關閉閥。在一實例中,氣流程式碼1 4 6係操作 質流控制器’以控制氣流流率,進而提供一錢鍍氣體,其中 該濺鍍氣體具有含氧氣體相對於氬氣在一第一時間週期下 之第一體積流率比例,與含氧氣體相對於氬氣在一第二時間 週期下之第二體積流率比例。 當執行排放控制程式碼1 4 7時,自處理室管理者程式碼 1 44接收一欲求之壓力層級而做為一參數。排放控制程式碼 147藉由讀取連接於處理室3 6a中之一或多個傳統壓力計(未 示於圖中),以測量處理室3 6 a内之壓力,並比較測量值與 乾材壓力’且由一相應於靶材壓力之已存壓力表獲得pID值 (比例’積分,與微分),再根據由壓力表所獲得之PID值 來調整排放系統28之節流閥37。另外,亦可調節排放系統 28之排氣管線34的節流閥37之開口尺寸,而來調節處理室 36a中之壓力。 選擇式加熱器控制程式碼1 48係包含用於控制加熱基板 25 1290341 之選擇式加 — 一^一·^二圖中)溫度之程式碼。加熱器控 制程式碼 ~-—__ 厭私山 '藉由測垔位於支撐件1 8内之一熱電耦之電 1輸出來測晉、、田痒 '胤又,w比較測量溫度與設定溫度之差異,以 曰加或減少施於加埶哭 .^ ^ …益之電流,進而獲得該欲求之升降速率 或叹疋溫度。續、、田诤尨奸 ,β μ度係可藉由檢閱存於換算表之對應溫度, 3 II由使用四階多式 輕 貝式计异而由測得壓力得知該溫度。當以 :燈作為加熱器時,加熱器控制程式碼148逐步地控制施 夕;於燈泡之電流的增減,以增加燈泡的壽命與可靠度。此 、°匕3嵌入式故障安全模式以檢測製程安全符合情 並富處理室36a尚未摘舍举抓拉 j. ^ 4. 禾週田架δ又時,係可用於關閉加熱器 的《ί呆作。 電壓源程式碼149包含用於控制電麗源之程式瑪,以在 室、36at激發賤鑛氣體’而自乾材14減鐘材料,其中 Μ電壓源諸如DC電壓源。舉例 於釦从, 程式碼149係設定施 、祀材14之脈衝Dc電壓層級,並也 側牆以 弋慝理至36 a中之 ° 之電性狀態。相似於先前所描述t θ > π m , ^ . 疋之處理室組件程式 程式碼1 4 9係藉由處理室管理者程式 在一 狂八碼144加以執行。 耜作冲,程式碼149含有之步驟係為··读 之『 々嗔取施於靶材14 问刖』功率與流經處理室36a之『s M c 射』功率。過高的 射功率讀取值即表示電漿未被點燃,此 新門H 此時程式碼149會重 開始或關閉該製程。將讀取的功率層級與 光抽& ’、犯柯層級比較, 龙調整該電流以控制電漿。 26 1290341 —代習知處理製程與塗覆 製程所得之增強的金一 -——一~ 在此實例中,根據本發明,包含氧化鋁之一陶瓷體302 係經處理並塗覆一含鋁之金屬塗層304。在一第一處理步驟 中,氧化鋁陶瓷體302之表面係以珠擊而形成一粗糙度^均 值為100微英对之表面。在-第二處理步驟中,氧化链陶曼 體3 02表面係持續一分鐘而沈浸於濃度為5體積百分比之含 鹽酸溶液中。利用雙絲熱噴塗法而將鋁金屬塗層3〇4塗佈至 已處理表面306,其中使用之雙鋁絲係視為消耗性電極。鋁 材料係喷塗至表面3〇6上,以形成厚度為〇 25mm之塗層3〇4。 鋁金屬塗層304與氧化鋁陶瓷體3〇2間之鍵結強度係經 判定後,與習知製程所製備得之組件3〇〇之鍵結強度相比 較。其中該鍵結強度係根據ASTM C633測試標準來判定。 在使用ASTM測試標準中,金屬塗層3〇4之表面3〇8係用一 黏著劑連接至一固定裝置(Hxture )。通過該固定裝置,則垂 直施加一拉伸負載於塗層304平面,以判定塗層之鍵結強 度。黏著或黏合強度程度係根據下列方程式加以決定: 1 ^黏著或黏合強度=最大負載/橫截面面積 第6圖係說明比較A-E組件之鍵結強度,其中標示為E 之組件係表示以本發明之方法加以處理與塗覆之組件3〇〇之 標準化鍵結強度,而標示為A_D之組件,係表示以習知方法 加以處理與塗覆之組件300之鍵結強度。如圖中所示,本製 程係提供一組件300,該組件300在塗層3〇4與陶瓷體3〇2 1290341 一鍵結。第i圖亦顯示,組件D之鍵結強 度低於本製程 c之鍵結強度低於組件Ε之鍵結強度之一半。 所量測之鍵結強度亦可用來估算組件300之部件壽命, 其係定義為需要去除或再磨光組# 300 1,可於處理室36a 中處理基板16之數量’以更確認根據本製程加以處理與塗 覆之組件300所增強之性能。組件A與B估算具有處理約 3〇〇〇片基板之部件壽命,組件c估算具有處理2〇〇〇_45〇〇片 基板之部件壽命,而組件D估算具有處理52〇〇_65〇〇個晶圓 之部件壽命。相較之下,以本製程所製備之組件E估算具有 處理至少約7500個晶圓之實質增加的部件壽命。 因此,經由本製程處理陶瓷體表面3〇6而製備的組件 3〇〇,係增強金屬塗層304與表面3〇6之鍵結,藉此增強金 屬塗層與陶瓷體之鍵結強度,並降低組件3〇〇中金屬塗層 瓷體302上傾向分層或剝離的機率。以本發明加以處理 ,塗覆之組件300,係改善基板製程環境之抗腐蝕性與延長 部件之壽命,因此增加處理基板16之效率與品質。 蓺雖然本發明已以前述較佳實施例揭示,然任何熟習此技 藝者,在不脫離本發明之精神和範圍内,所製造之其他實施 例丄亦併入本發明之範圍。舉例而言,係可用其他處理劑取 代别述所提之實例。同樣地,如熟習此技藝者熟知的,陶瓷 ,302與金屬塗層3〇4係可包含其他替代之組成。此外,參 照本發明圖中所示之較佳實施例之位置關係,係可為之下、 之上、底冑、頂部、向上、向下、第一與第二與其他相關位 28 1290341 且此關係係可^ 此,後附申請專|从 配置。 何抖、或空間 L園式 經 以說明 於瞭解 僅偈限 組合, 第1圖 第2圖 第3圖 第4圖 第5圖 第6圖 簡單說明】 由以下之描述、後附之專利申請範圍與所 J 圖 7|Τ 力口 本發明之實例,以使本發明之特徵、觀點與優點 。然而,一般可使用於本發明中之每一特徵,卷=易 於本文中之特定圖#’本發明尚包括此類特徵::: 其中: 仕忍 為具有-金屬塗層之處理室組件之截面側視圖。 為根據本發明一實施例之製程流程圖。 為-裝置之實施例之截面上視圖,其中該裝置包人—a process chamber component 300; determining a component to be operated 300 based on process parameters to be executed by the process; and executing a process component code corresponding to the monitoring and decision step. The operation of a particular process room component code will now be described. The substrate positioning code 145 includes code for controlling the process chamber assembly 3, wherein the assembly 300 is used to transport a substrate 16 onto the substrate support 18, and optionally the substrate is disposed in the processing chamber 36. 1 6 liters are lifted to the desired height to control the distance between the substrate 16 and the target. When the substrate 16 is transferred into the processing chamber, the substrate support 18 is lowered to receive the substrate 16, and then the support member 上升 rises to the desired height in the processing chamber 36a. The substrate positioning code 145 controls the displacement of the support member 18 in response to process setting parameters from the process chamber manager code 44 regarding the height of the support member. Airflow code 146 is used to control process composition and flow rate. The gas conduit 34, which is typically used for each process, includes a safety shut-off valve (not shown) that automatically or manually shuts down the process gas flow into the process chamber 36a. When a toxic gas is used in the process, the "death" phase is located on each of the gas conduits 34. The airflow code 1 4 6 controls the on/off state of the safety shutdown threshold and causes the mass flow controller to accelerate/decelerate at the flow rate. The airflow code 1 46, like all of the process room component code, is executed by the process room manager code 144 and is processed by the process manager code 14 14 for process parameters relating to the desired gas flow rate. The operation of the airflow code 1 4 6 is generally adjusted by repeatedly reading the necessary mass flow controller, comparing the read value with the desired flow rate received to the manager code 144, and then adjusting as needed. Flow rate. In addition, the airflow code 146 includes steps to monitor an unsafe airflow rate and initiate a safety shut-off valve when an unsafe condition is detected. In one example, the airflow code 146 operates the mass flow controller to control the airflow rate to provide a gas plating gas, wherein the sputtering gas has an oxygen-containing gas relative to argon for a first period of time The first first volumetric flow rate ratio is proportional to the second volumetric flow rate of the oxygen-containing gas relative to the argon gas over a second period of time. When the emission control code 1 4 7 is executed, the processing chamber manager code 1 44 receives a desired pressure level as a parameter. The emission control code 147 measures the pressure in the processing chamber 3 6 a by reading one or more conventional pressure gauges (not shown) connected to the processing chamber 36a, and compares the measured values with the dry materials. The pressure 'and the pID value (proportional 'integral, and differential') is obtained from an existing pressure gauge corresponding to the target pressure, and the throttle valve 37 of the discharge system 28 is adjusted based on the PID value obtained from the pressure gauge. Alternatively, the opening size of the throttle valve 37 of the exhaust line 34 of the exhaust system 28 can be adjusted to adjust the pressure in the process chamber 36a. The Selective Heater Control Code 1 48 series contains code for controlling the temperature of the heating substrate 25 1290341 in the selection plus one. Heater control code ~--__ 厌私山' by measuring the electric 1 output of a thermocouple located in the support member 18 to measure Jin, tian itch '胤, w compare temperature and set temperature The difference is to increase or decrease the current applied to the coronation, and then to obtain the desired rate of rise or fall or the temperature of the sigh. Continued, Tian Tian rape, β μ degree can be checked by the corresponding temperature stored in the conversion table, 3 II is determined by the measured pressure using the fourth-order multi-style light-shell type. When the lamp is used as the heater, the heater control code 148 gradually controls the temperature of the lamp to increase or decrease the current of the lamp to increase the life and reliability of the lamp. This, ° 匕 3 embedded fail-safe mode to detect process safety compliance and rich processing room 36a has not been picked up and pulled j. ^ 4. He Zhou Tian δ again, can be used to turn off the heater Work. The voltage source code 149 contains a program for controlling the source of the battery to excite the strontium gas in the chamber, 36 volts to depress the material from the dry material 14, and a voltage source such as a DC voltage source. For example, the deduction, the code 149 sets the pulse Dc voltage level of the application and the coffin 14, and also the side wall is treated to the electrical state of the temperature of 36 a. Similar to the previously described t θ > π m , ^ . The processing room component program code 1 4 9 is executed by the processing room manager program in a mad eight code 144. In the case of the code 149, the step 149 includes the reading of the "power applied to the target 14" and the "s M c" power flowing through the processing chamber 36a. Excessive reading power reading means that the plasma is not ignited. This new door H will restart or close the process at 149. The read power level is compared to the light pumping &', and the level is adjusted to control the plasma. 26 1290341 - Reinforced gold----in this example, in accordance with the present invention, a ceramic body 302 comprising alumina is treated and coated with an aluminum-containing Metal coating 304. In a first processing step, the surface of the alumina ceramic body 302 is beaded to form a surface having a roughness of 100 micro-pairs. In the second treatment step, the surface of the oxidized chain Tauman 3 02 was continued for one minute and immersed in a hydrochloric acid solution having a concentration of 5 volume percent. The aluminum metal coating 3〇4 was applied to the treated surface 306 by a two-wire thermal spraying method in which the double aluminum wire system was used as a consumable electrode. The aluminum material was sprayed onto the surface 3〇6 to form a coating 3〇4 having a thickness of 25 mm. The bonding strength between the aluminum metal coating 304 and the alumina ceramic body 3〇2 is judged to be compared with the bonding strength of the assembly 3 prepared by the conventional process. Wherein the bond strength is determined according to the ASTM C633 test standard. In the ASTM test standard, the surface 3〇8 of the metal coating 3〇4 is attached to a fixture (Hxture) with an adhesive. By means of the fixture, a tensile load is applied vertically to the plane of the coating 304 to determine the bonding strength of the coating. The degree of adhesion or adhesion strength is determined according to the following equation: 1 ^ Adhesion or bond strength = maximum load / cross-sectional area Figure 6 is a comparison of the bond strength of the AE component, wherein the component labeled E is represented by the present invention. The method is to treat the standardized bond strength of the coated component 3, and the component labeled A_D represents the bond strength of the component 300 treated and coated by conventional methods. As shown in the figure, the process provides an assembly 300 that is bonded to the ceramic body 3〇2 1290341 at a coating 3〇4. The figure i also shows that the bonding strength of the component D is lower than that of the process c, and the bonding strength is lower than one and a half of the bonding strength of the component Ε. The measured bond strength can also be used to estimate the component life of the component 300, which is defined as the need to remove or re-polish the group #3001, which can process the number of substrates 16 in the process chamber 36a to further confirm the process according to the process. The enhanced performance of the coated assembly 300 is treated. Components A and B are estimated to have a component life of approximately 3 基板 substrate, component c is estimated to have a component life of 2 〇〇〇 45 substrates, and component D is estimated to have a process of 52 〇〇 _65 〇〇 The life of the components of a wafer. In contrast, component E prepared in this process is estimated to have a substantially increased component lifetime for processing at least about 7,500 wafers. Therefore, the assembly 3〇〇 prepared by treating the surface 3′6 of the ceramic body through the process enhances the bonding of the metal coating 304 and the surface 3〇6, thereby enhancing the bonding strength between the metal coating and the ceramic body, and The probability of delamination or peeling on the metal coated porcelain 302 in the assembly 3〇〇 is reduced. The assembly 300 is treated by the present invention to improve the corrosion resistance of the substrate process environment and extend the life of the component, thereby increasing the efficiency and quality of the substrate 16. Although the present invention has been disclosed in the foregoing preferred embodiments, other embodiments of the invention may be made without departing from the spirit and scope of the invention. For example, other treatment agents may be substituted for the examples described. Likewise, as is well known to those skilled in the art, the ceramic, 302 and metal coated 3〇4 series may comprise other alternative compositions. Furthermore, reference is made to the positional relationship of the preferred embodiment shown in the figures of the present invention, which may be lower, upper, lower, top, upward, downward, first and second and other related bits 28 1290341 and this The relationship can be ^, followed by the application | from the configuration. He shakes, or space L garden type to illustrate the only limited combination, Figure 1 Figure 2 Figure 3 Figure 4 Figure 5 Figure 6 is a brief description] The following description, attached patent application scope And the examples of the present invention are made to make the features, viewpoints and advantages of the present invention. However, it is generally possible to use each of the features in the present invention, volume = easy to be specific in the text herein. The present invention also includes such features:: where: 仕忍 is a cross section of a process chamber component having a metal coating Side view. A process flow diagram in accordance with an embodiment of the present invention. A cross-sectional upper view of an embodiment of the device, wherein the device is packaged -
多重處理室平台,該平台上係包括有相互連結之PVD 處理室。 為較佳卿處理室之一實施例之戴面側視圖。 為-電腦程式實施例的層次控制架構之簡化方塊圖, 其中該電腦程式具有操作第4圖_處理室之能力。 為-柱狀圖,係比較以不同製程製造之組件上的金屬 塗層之鍵結強度。 【元件代表符號簡單說明】 12 (處理室圍繞)牆 13頂板 29 1290341 14靶材 15 沉積環 16基板 17覆蓋環 18支撐件 19表面 20屏蔽 22 電源 23 氣體供應器 24氣體源 25a,b氣體輸入 26質流控制器 27氣體源 28 (氣體)排放系統 29排氣口 30控制器 31混合岐管 32磁控管 33 氣體入口 34排氣管線/氣體導管 3 5磁場產生器 36a (PVD)處理室 36b 處理室 36c處理室 1290341 36d處理室 3 7節流閥 38 電漿區域 39氣體分散器 45側牆 78旋轉軸 90氣體激發器 98磁性軛鐵 100平台 102冷卻處理室 104軸 105磁場 106 馬達 11 4預清洗處理室 11 8除氣處理室 120加載鎖定處理室 122加載鎖定處理室 126傳送匣 132機械臂裝置 134葉片 136 (製程)程序裝置 1 41電腦程式產品 142〜149 程式碼 3 00組件 1290341 302 陶瓷體 304 塗層 306表面 308 表面A multi-processing chamber platform that includes interconnected PVD processing chambers. A side view of a wear side of an embodiment of a preferred processing chamber. A simplified block diagram of a hierarchical control architecture for a computer program embodiment, wherein the computer program has the ability to operate Figure 4 - Processing Room. A - histogram compares the bond strength of a metal coating on a component manufactured in a different process. [Simple description of component symbol] 12 (processing room surrounding) wall 13 top plate 29 1290341 14 target 15 deposition ring 16 substrate 17 cover ring 18 support 19 surface 20 shield 22 power supply 23 gas supply 24 gas source 25a, b gas input 26 mass flow controller 27 gas source 28 (gas) exhaust system 29 exhaust port 30 controller 31 mixing manifold 32 magnetron 33 gas inlet 34 exhaust line / gas conduit 3 5 magnetic field generator 36a (PVD) processing chamber 36b processing chamber 36c processing chamber 1209034 36d processing chamber 3 7 throttle valve 38 plasma region 39 gas disperser 45 side wall 78 rotating shaft 90 gas energizer 98 magnetic yoke 100 platform 102 cooling processing chamber 104 shaft 105 magnetic field 106 motor 11 4 pre-cleaning processing chamber 11 degassing processing chamber 120 loading locking processing chamber 122 loading locking processing chamber 126 conveying 匣 132 robot arm device 134 blade 136 (process) program device 1 41 computer program product 142~149 code 3 00 component 1129034 302 ceramic body 304 coating 306 surface 308 surface
Claims (1)
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US10/032,387 US6656535B2 (en) | 2001-12-21 | 2001-12-21 | Method of fabricating a coated process chamber component |
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TW200305934A TW200305934A (en) | 2003-11-01 |
TWI290341B true TWI290341B (en) | 2007-11-21 |
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TW091134128A TWI290341B (en) | 2001-12-21 | 2002-11-22 | Method of fabricating a coated process chamber component |
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US (1) | US6656535B2 (en) |
EP (1) | EP1358666A1 (en) |
JP (1) | JP2005514521A (en) |
KR (1) | KR100951338B1 (en) |
CN (1) | CN1294615C (en) |
MY (1) | MY130996A (en) |
TW (1) | TWI290341B (en) |
WO (1) | WO2003058672A1 (en) |
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-
2002
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- 2002-11-19 JP JP2003558891A patent/JP2005514521A/en not_active Withdrawn
- 2002-11-19 CN CNB02806156XA patent/CN1294615C/en not_active Expired - Fee Related
- 2002-11-19 WO PCT/US2002/037219 patent/WO2003058672A1/en not_active Application Discontinuation
- 2002-11-19 KR KR1020037011452A patent/KR100951338B1/en not_active IP Right Cessation
- 2002-11-22 TW TW091134128A patent/TWI290341B/en not_active IP Right Cessation
- 2002-12-20 MY MYPI20024830A patent/MY130996A/en unknown
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KR20040063792A (en) | 2004-07-14 |
KR100951338B1 (en) | 2010-04-08 |
TW200305934A (en) | 2003-11-01 |
CN1496577A (en) | 2004-05-12 |
US6656535B2 (en) | 2003-12-02 |
EP1358666A1 (en) | 2003-11-05 |
CN1294615C (en) | 2007-01-10 |
US20030118731A1 (en) | 2003-06-26 |
WO2003058672A1 (en) | 2003-07-17 |
MY130996A (en) | 2007-07-31 |
JP2005514521A (en) | 2005-05-19 |
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